Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 9 de 9
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
New Phytol ; 243(2): 720-737, 2024 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-38812277

RESUMO

During arbuscular mycorrhizal (AM) symbiosis, plant innate immunity is modulated to a prime state to allow for fungal colonization. The underlying mechanisms remain to be further explored. In this study, two rice genes encoding LysM extracellular (LysMe) proteins were investigated. By obtaining OsLysMepro:GUS transgenic plants and generating oslysme1, oslysme2 and oslysme1oslysme2 mutants via CRISPR/Cas9 technique, OsLysMe genes were revealed to be specifically induced in the arbusculated cells and mutations in either gene caused significantly reduced root colonization rate by AM fungus Rhizophagus irregularis. Overexpression of OsLysMe1 or OsLysMe2 dramatically increased the colonization rates in rice and Medicago truncatula. The electrophoretic mobility shift assay and dual-luciferase reporter assay supported that OsLysMe genes are regulated by OsWRI5a. Either OsLysMe1 or OsLysMe2 can efficiently rescue the impaired AM phenotype of the mtlysme2 mutant, supporting a conserved function of LysMe across monocotyledonous and dicotyledonous plants. The co-localization of OsLysMe proteins with the apoplast marker SP-OsRAmy3A implies their probable localization to the periarbuscular space (PAS) during symbiosis. Relative to the fungal biomass marker RiTEF, some defense-related genes showed disproportionately high expression levels in the oslysme mutants. These data support that rice plants deploy two OsLysMe proteins to facilitate AM symbiosis, likely by diminishing plant defense responses.


Assuntos
Regulação da Expressão Gênica de Plantas , Mutação , Micorrizas , Oryza , Proteínas de Plantas , Simbiose , Micorrizas/fisiologia , Oryza/microbiologia , Oryza/genética , Proteínas de Plantas/metabolismo , Proteínas de Plantas/genética , Mutação/genética , Plantas Geneticamente Modificadas , Medicago truncatula/microbiologia , Medicago truncatula/genética , Motivos de Aminoácidos , Espaço Extracelular/metabolismo , Raízes de Plantas/microbiologia , Raízes de Plantas/metabolismo , Fungos
2.
Mol Psychiatry ; 28(9): 3955-3965, 2023 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-37798418

RESUMO

Diabetic patients receiving the antidiabetic drug metformin have been observed to exhibit a lower prevalence of anxiety disorders, yet the precise mechanism behind this phenomenon is unclear. In our study, we found that anxiety induces a region-specific reduction in AMPK activity in the medial prefrontal cortex (mPFC). Concurrently, transgenic mice with brain-specific AMPK knockout displayed abnormal anxiety-like behaviors. Treatment with metformin or the overexpression of AMPK restored normal AMPK activity in the mPFC and mitigated social stress-induced anxiety-like behaviors. Furthermore, the specific genetic deletion of AMPK in the mPFC not only instigated anxiety in mice but also nullified the anxiolytic effects of metformin. Brain slice recordings revealed that GABAergic excitation and the resulting inhibitory inputs to mPFC pyramidal neurons were selectively diminished in stressed mice. This reduction led to an excitation-inhibition imbalance, which was effectively reversed by metformin treatment or AMPK overexpression. Moreover, the genetic deletion of AMPK in the mPFC resulted in a similar defect in GABAergic inhibitory transmission and a consequent hypo-inhibition of mPFC pyramidal neurons. We also generated a mouse model with AMPK knockout specific to GABAergic neurons. The anxiety-like behaviors in this transgenic mouse demonstrated the unique role of AMPK in the GABAergic system in relation to anxiety. Therefore, our findings suggest that the activation of AMPK in mPFC inhibitory neurons underlies the anxiolytic effects of metformin, highlighting the potential of this primary antidiabetic drug as a therapeutic option for treating anxiety disorders.


Assuntos
Ansiolíticos , Metformina , Humanos , Camundongos , Animais , Ansiolíticos/farmacologia , Proteínas Quinases Ativadas por AMP/farmacologia , Metformina/farmacologia , Hipoglicemiantes/farmacologia , Córtex Pré-Frontal , Neurônios GABAérgicos
3.
Zhongguo Zhen Jiu ; 43(6): 691-6, 2023 Jun 12.
Artigo em Chinês | MEDLINE | ID: mdl-37313564

RESUMO

The scientific basis of acupuncture on mesenchymal stem cells (MSCs) for treating ischemic stroke (IS) is discussed. MSCs transplantation has great potential for the treatment of tissue damage caused by early stage inflammatory cascade reactions of IS, but its actual transformation is limited by various factors. How to improve the homing efficiency of MSCs is the primary issue to enhance its efficacy. As such, the possible mechanisms of acupuncture and MSCs transplantation in inhibiting inflammatory cascade reactions induced by IS are explored by reviewing literature, and a hypothesis that acupuncture could promote the secretion of stromal cell-derived factor-1α (SDF-1α) from ischemic foci to regulate SDF-1α/CXC chemokine receptor 4 (CXCR4) axis, thereby improving the homing efficiency of MSCs transplantation, exerting its neuroprotective function, and improving the bed transformation ability, is proposed.


Assuntos
Terapia por Acupuntura , AVC Isquêmico , Células-Tronco Mesenquimais , Humanos , Quimiocina CXCL12 , Inflamação
4.
Zhongguo Shi Yan Xue Ye Xue Za Zhi ; 30(3): 744-749, 2022 Jun.
Artigo em Chinês | MEDLINE | ID: mdl-35680799

RESUMO

OBJECTIVE: To explore the expression of cellular apoptosis susceptibility protein (CAS) in acute myeloid leukemia (AML) and its correlation with clinical characteristics. METHODS: The expression of CAS in bone marrow tissue of 54 patients with AML and 24 patients with non-hematological malignant diseases was detected by Western blot and immune-histochemical method, and compared between AML group and control group. Also the relationship of CAS expression in AML and sex, age, WBC count, Hb, platelet count, bone marrow blast cell ratio, ki-67 index, cytogenetic and molecular biological prognostic risk stratification, extramedullary infiltration and other clinical characteristics was analyzed. RESULTS: Western blot showed that the expression of CAS protein in bone marrow biopsies of AML patients was significantly higher than that in control group (P<0.05). Immune-histochemical method revealed that CAS was mainly located in the cytoplasm in both AML group and control group. Among 54 AML patients, 14 patients (25.9%) showed high expression of CAS, while all the 24 patients in the control group showed low expression of CAS. The high expression rate of CAS in AML patients was significantly higher than that in the control group (P<0.05). There were statistically significant differences in prognostic risk stratification and the remission rate of the first chemotherapy between CAS high expression group and CAS low expression group in AML (P<0.05). The proportion of high risk patients and unremission patients after the first chemotherapy in CAS high expression group were significantly higher than those in CAS low expression group (57.1% vs 27.5%, 30.8% vs 7.9%), while the proportion of low risk patients and complete remission patients after the first chemotherapy were significantly lower than those in CAS low expression group (14.3% vs 37.5%, 53.8% vs 84.2%). In AML patients, the ki-67 index of bone marrow tissue in CAS high expression group was higher than that in CAS low expression group (60% vs 50%) (P<0.05). CONCLUSION: CAS is localized in cytoplasm in both AML and non-hematological malignant diseases, and its expression increases in AML. CAS is related to the risk stratification of cytogenetics and molecular biology, the remission rate after the first chemotherapy and ki-67 index in AML, which suggests that CAS may be involved in the occurrence and development of AML.


Assuntos
Proteína de Suscetibilidade a Apoptose Celular , Leucemia Mieloide Aguda , Medula Óssea/metabolismo , Proteína de Suscetibilidade a Apoptose Celular/metabolismo , Humanos , Antígeno Ki-67/metabolismo , Leucemia Mieloide Aguda/tratamento farmacológico , Prognóstico , Indução de Remissão
5.
Sci Total Environ ; 838(Pt 3): 156405, 2022 Sep 10.
Artigo em Inglês | MEDLINE | ID: mdl-35660601

RESUMO

To examine the perturbation of atmospheric nitrogen (N) deposition on soil N status and the biogeochemical cycle is meaningful for understanding forest function evolution with environmental changes. However, levels of soil bioavailable N and their environmental controls in forests receiving high atmospheric N deposition remain less investigated, which hinders evaluating the effects of enhanced anthropogenic N loading on forest N availability and N losses. This study analyzed concentrations of soil extractable N, microbial biomass N, net rates of N mineralization and nitrification, and their relationships with environmental factors among 26 temperate forests under the N deposition rates between 28.7 and 69.0 kg N ha-1 yr-1 in the Beijing-Tianjin-Hebei (BTH) region of northern China. Compared with other forests globally, forests in the BTH region showed higher levels of soil bioavailable N (NH4+, 27.1 ± 0.8 mg N kg-1; NO3-, 7.0 ± 0.8 mg N kg-1) but lower net rates of N mineralization and nitrification (0.5 ± 0.1 mg N kg-1 d-1 and 0.4 ± 0.1 mg N kg-1 d-1, respectively). Increasing N deposition levels increased soil nitrification and NO3- concentrations but did not increase microbial biomass N and N mineralization among the study forests. Soil moisture and C availability were found as dominant factors influencing microbial N mineralization and bioavailable N. In addition, by budgeting the differences in soil total N densities between the 2000s and 2010s, atmospheric N inputs to the forests were more retained in soils than lost proportionally (84% vs. 16%). We concluded that the high N deposition enriched soil N without stimulating microbial N mineralization among the study forests. These results clarified soil N status and the major controlling factors under high anthropogenic N loading, which is helpful for evaluating the fates and ecological effects of atmospheric N pollution.


Assuntos
Nitrogênio , Solo , China , Florestas , Nitrificação , Nitrogênio/análise , Microbiologia do Solo
6.
Complement Ther Clin Pract ; 40: 101210, 2020 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-32891286

RESUMO

BACKGROUND: and purpose: We investigated the effectiveness of cupping therapy with three different pressures in patients with chronic fatigue syndrome (CFS). MATERIALS AND METHODS: The participants were randomly assigned to three groups, as follows: cupping pressure of -0.02 mpa (n = 38), -0.03 mpa (n = 38), or -0.05 mpa (n = 36). Each group received cupping treatment that consisted of 10 sessions over 5 weeks (2 sessions per week). The primary outcomes were Fatigue Scale (FS-14) score and Fatigue Assessment Instrument (FAI) score after 5 and 10 sessions. The secondary outcomes were the Self-Rating Anxiety Scale (SAS) score, the Self-Rating Depression Scale (SDS) score, and the Pittsburgh Sleep Quality Index (PSQI) score. RESULTS: There were 91 participants who completed the trial. After five sessions of treatment, the primary outcome of FS-14 score decreased by 3.20 (2.19, 4.21) in the -0.02 mpa group, by 2.39 (1.51, 3.27) in the -0.03 mpa group, and by 3.40 (2.28, 4.52) in the -0.05 mpa group (P = 0.667). After 10 sessions of treatment, the outcome of FS-14 score decreased by 5.00 (3.79, 6.21) in the -0.02 mpa group, by 4.06 (3.07, 5.05) in the -0.03 mpa group, and by 4.77 (3.52, 5.94) in the -0.05 mpa group (P = 0.929). And, the results were statistically different between 5 sessions and 10 sessions of treatment (P < 0.01). However, there were no statistical differences in FAI, SAS, SDS, and PSQI scores between the three groups after 5 sessions and 10 sessions of treatment. CONCLUSIONS: In conclusion, cupping therapy has significantly relieved fatigue symptoms and improved emotion and sleep condition of CFS patients, and 10 sessions of treatment had superior results compared with 5 sessions in each group. Moreover, in 5 sessions of treatment, cupping with high pressure showed better improvement in fatigue syndromes and sleep condition according to effective rates. TRIAL REGISTRATION: Chinese clinical trial registry (ChiCTR1800017590); Ethical approval number: ChiECRCT-20180085.


Assuntos
Ventosaterapia/métodos , Síndrome de Fadiga Crônica/terapia , Adulto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Método Simples-Cego , Transtornos do Sono-Vigília/terapia , Adulto Jovem
7.
World J Gastroenterol ; 26(32): 4802-4816, 2020 Aug 28.
Artigo em Inglês | MEDLINE | ID: mdl-32921958

RESUMO

BACKGROUND: Multiple sites of metastasis and desmoplastic reactions in the stroma are key features of human pancreatic cancer (PC). There are currently no simple and reliable animal models that can mimic these features for accurate disease modeling. AIM: To create a new xenograft animal model that can faithfully recapitulate the features of human PC. METHODS: Interleukin 2 receptor subunit gamma (IL2RG) gene knockout Syrian hamster was created and characterized. A panel of human PC cell lines were transplanted into IL2RG knockout Syrian hamsters and severe immune-deficient mice subcutaneously or orthotopically. Tumor growth, local invasion, remote organ metastasis, histopathology, and molecular alterations of tumor cells and stroma were compared over time. RESULTS: The Syrian hamster with IL2RG gene knockout (named ZZU001) demonstrated an immune-deficient phenotype and function. ZZU001 hamsters faithfully recapitulated most features of human PC, in particular, they developed metastasis at multiple sites. PC tissues derived from ZZU001 hamsters displayed desmoplastic reactions in the stroma and epithelial to mesenchymal transition phenotypes, whereas PC tissues derived from immune-deficient mice did not present such features. CONCLUSION: ZZU001 hamsters engrafted with human PC cells are a superior animal model compared to immune-deficient mice. ZZU001 hamsters can be a valuable animal model for better understanding the molecular mechanism of tumorigenesis and metastasis and the evaluation of new drugs targeting human PC.


Assuntos
Transição Epitelial-Mesenquimal , Neoplasias Pancreáticas , Animais , Cricetinae , Modelos Animais de Doenças , Xenoenxertos , Humanos , Mesocricetus , Camundongos , Neoplasias Pancreáticas/genética
8.
Sci Total Environ ; 713: 136620, 2020 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-32019017

RESUMO

Human activities have distinctly enhanced the deposition levels of atmospheric nitrogen (N) pollutants into terrestrial ecosystems, but whether and to what extents soil carbon (C) and N status have been influenced by elevated N inputs remain poorly understood in the 'real' world given related knowledge has largely based on N-addition experiments. Here we reported soil organic C (OC) and total N (TN) for twenty-seven forests along a gradient of N deposition (22.4-112.9 kg N/ha/yr) in the Beijing-Tianjin-Hebei (BTH) region of northern China, a global hotspot of high N pollution. Levels of soil TN in forests of the BTH region have been elevated compared with investigations in past decades, suggesting that long-term N deposition might cause soil TN increases. Combining with major geographical and environmental factors among the study forests, we found unexpectedly that soil moisture and pH values rather than N deposition levels were major regulators of the observed spatial variations of soil OC and TN contents. As soil moisture and pH values increased with mean annual precipitation and temperature, respectively, soil C and N status in forests of the BTH region might be more responsive to climate change than to N pollution. These evidence suggests that both N deposition and climate differences should be considered into managing ecosystem functions of forest resources in regions with high N pollution.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...